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DAYE (ANNE'S DAY LTD) Recalls

29 recalls on record · November 5, 2025 to November 5, 2025 · Medical Devices

November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month Heavy Flow Bundle; Model Number: FG-BNDL-PC-MM-IBHF;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month Regular Flow Bundle; Model Number: FG-BNDL-PC-MM-IBRF;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month All in One Bundle; Model Number: FG-BNDL-PC-MM-IBAIO;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-IB09090909;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Initiation 18 Coated Super and 18 Nude Super Tampons; Model Number: FG-TMP-MM-IB00180018;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Initiation 18 Coated Regular and 18 Nude Regular Tampons; Model Number: FG-TMP-MM-IB18001800;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Initiation 18 Coated Regular and 18 Coated Super Tampons; Model Number: FG-TMP-MM-IB18180000;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Initiation 36 Coated Super Tampons; Model Number: FG-TMP-MM-IB00360000;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Initiation 36 Coated Regular Tampons; Model Number: FG-TMP-MM-IB36000000;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Refill 3 Month Heavy Flow Bundle; Model Number: FG-BNDL-PC-MM-REFHF;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Refill 3 Month Regular Flow Bundle; Model Number: FG-BNDL-PC-MM-REFRF;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Refill 3 Month All in One Bundle; Model Number: FG-BNDL-PC-MM-REFAIO;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Refill 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-REF09090909;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Refill 18 Coated Super and 18 Nude Super Tampons; Model Number: FG-TMP-MM-REF00180018;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Refill 18 Coated Regular and 18 Nude Regular Tampons; Model Number: FG-TMP-MM-REF18001800;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Refill 18 Coated Regular and 18 Coated Super Tampons; Model Number: FG-TMP-MM-REF18180000;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Refill 36 Coated Super Tampons; Model Number: FG-TMP-MM-REF00360000;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Refill 36 Coated Regular Tampons; Model Number: FG-TMP-MM-REF36000000;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Heavy Flow Bundle; Model Number: FG-BNDL-PC-REFHF;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Regular Flow Bundle; Model Number: FG-BNDL-PC-REFRF;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls All in One Bundle; Model Number: FG-BNDL-PC-REFAIO;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls Trial Tampon Box; Model Number: FG-TMP-REF04050504;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls 9 Coated Super and 9 Nude Super Tampons; Model Number: FG-TMP-REF00090009;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls 9 Coated Regular and 9 Nude Regular Tampons; Model Number: FG-TMP-REF09000900;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls 9 Coated Regular and 9 Coated Super Tampons; Model Number: FG-TMP-REF09090000;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls 18 Coated Super Tampons; Model Number: FG-TMP-REF00180000;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls 18 Coated Regular Tampons; Model Number: FG-TMP-REF18000000;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls 9 Coated Regular Tampons and 9 Nude Regular Tampons; Model Number: FG-TMP-RET09000900;
Hazard: Product lacks 510(k) clearance.
November 5, 2025Medical DevicesFDA
DAYE (ANNE'S DAY LTD) recalls 9 Coated Super Tampons and 9 Nude Super Tampons; Model Number: FG-TMP-RET00090009;
Hazard: Product lacks 510(k) clearance.
DAYE (ANNE'S DAY LTD) Recalls | RecallWatchUSA